# K063448: Emg AC/DC Suction Unit

- Pathway: 510(k) (Traditional)
- Applicant: Emg Technology Co., Ltd.
- Decided: Nov 30, 2006 after 15 days
- Product code: JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 878.4780
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K935218 (1994). 2 ancestors in all.
16 later devices descend from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982304: Devilbiss Suction Unit, Sunrise Medical Hhg, Inc. (1998) Summary page 1.

## Most influential descendants
- K082762: Aardvark Nasal Irrigation and Aspiration Device (2008), 15 descendants of its own
- K090379: Avita Nasal Aspirator, Model, NS1 Series (2010), 13 descendants of its own
- K180863: FORA NAS100 Electronic Nasal Aspirator, Electronic Nasal Aspirator (2018), 10 descendants of its own
- K222547: Electric nasal aspirator (2022), 9 descendants of its own
- K233901: Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008, NASA009) (2024), 3 descendants of its own

## Indications for use
The device is a vacuum suction device. It is to be used to remove infectious materials from wounds or fluids from a patient's airway or respiratory. It is for use on the order of a physician only.

Source page: https://510kreport.com/device/K063448
Methodology: https://510kreport.com/methodology